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Single Nucleotide Polymorphisms (SNPs) are among the most significant genetic markers used in genomics for identifying genetic variation. With the rapid growth of next-generation sequencing (NGS) technologies, the ability to detect and analyze SNPs has become essential in medical research, agricultural biotechnology, and evolutionary studies.
This workshop will dive deep into the process of SNP identification using actual NGS datasets, guiding participants through modern computational pipelines. Participants will learn data preprocessing, variant calling using Galaxy tools, visualization using Integrated Genomics Viewer (IGV), and foundational concepts in Genome-Wide Association Studies (GWAS). Ideal for those looking to transition into genomics, bioinformatics, and precision medicine, the workshop also highlights tools that work on Linux systems and how to set them up via Windows Subsystem for Linux (WSL).
This 3-day deep tech workshop aims to provide hands-on training in SNP detection using NGS data, familiarize participants with real-world tools like Galaxy and GATK pipelines, and equip them with bioinformatics techniques for variant analysis.
PhD in Computational Mechanics from MIT with 15+ years of experience in Industrial AI. Former Lead Data Scientist at Tesla and current advisor to Fortune 500 manufacturing firms.
Professional Certification Program
Understand the principles and significance of SNPs in genomics
Perform hands-on SNP identification using real-world NGS data
Use bioinformatics tools like Galaxy, IGV, and GATK for variant analysis
Learn data preprocessing and quality control of NGS reads
Explore SNP databases and interpret results for downstream applications
Day 1:
Introduction to SNPs and their biological significance
SNP identification using NGS data
Real-world applications and case studies
Exploration of SNP databases and GWAS overview
Day 2:
Fetching and preprocessing NGS datasets
Hands-on session with SNP detection tools
Basics of data quality control and error correction
Day 3:
Using Galaxy tools for SNP detection
Visualizing variants in IGV
Understanding and implementing the GATK pipeline
Final Q&A, certificate distribution
Workshop Prerequisite – PC with linux operating system or linux subsystem can be installed in windows
https://www.public-health.uiowa.edu/it/support/kb48549/
2025-06-27
Indian Standard Timing 2:00 PM
2025-06-27 to 2025-06-29
Indian Standard Timing 3:00 PM
Genomics & NGS-based Research Labs
Biotechnology and Pharma Companies
Precision Medicine Startups
Public Health and Cancer Genomics Programs
AI-powered Medical Diagnostics Firms
Academic & Industrial R&D Projects
INR. 2699
USD. 75
Bioinformatics Analyst in pharmaceutical companies
Research Scientist in genomics and medical diagnostics
Genomic Data Analyst in agritech companies
GWAS Researcher for academic/industrial studies
Personalized Medicine Expert
Clinical Bioinformatics Specialist in healthcare AI startups
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